Canonical Allele Identifier: CA1583144561
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393772C= , CM000667.2:g.132393772C= GRCh38
NC_000005.9:g.131729464C= , CM000667.1:g.131729464C= GRCh37
NC_000005.8:g.131757363C= NCBI36
NG_008982.1:g.29064C=
NG_008982.2:g.29069C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-413C= ENSP00000388838.2:n.1292-413C=
ENST00000435065.7:c.1619C= ENSP00000402760.2:p.Pro540=
ENST00000448810.6:c.*399C= ENSP00000401860.2:n.*399C=
ENST00000685543.1:n.1688C=
ENST00000686757.1:c.*711C= ENSP00000510721.1:n.*711C=
ENST00000686868.1:n.539C=
ENST00000687740.1:n.4232C=
ENST00000688151.1:n.2857C=
ENST00000689271.1:c.1394C= ENSP00000510797.1:p.Pro465=
ENST00000690900.1:c.*711C= ENSP00000510703.1:n.*711C=
ENST00000692212.1:n.4687C=
ENST00000692355.1:c.800C=
ENST00000692413.1:c.1529C= ENSP00000509374.1:p.Pro510=
ENST00000692825.1:c.1615C= ENSP00000509447.1:n.1615C=
ENST00000693308.1:c.1595C= ENSP00000509770.1:p.Pro532=
ENST00000693763.1:n.2707C=
ENST00000245407.8:c.1547C= MANE Select ENSP00000245407.3:p.Pro516=
ENST00000245407.7:c.1547C= ENSP00000245407.3:p.Pro516=
ENST00000435065.6:c.1619C= ENSP00000402760.2:p.Pro540=
ENST00000447841.5:c.391C=
ENST00000448810.5:c.809C=
ENST00000461013.5:n.8969C=
ENST00000475308.1:n.2225C=
NM_001308122.1:c.1619C= NP_001295051.1:p.Pro540=
NM_003060.3:c.1547C= NP_003051.1:p.Pro516=
XM_011543590.1:c.929C= XP_011541892.1:p.Pro310=
XR_948290.1:n.1673C=
XM_011543590.2:c.929C= XP_011541892.1:p.Pro310=
XM_017009778.2:c.1019C= XP_016865267.1:p.Pro340=
XR_001742215.1:n.1802C=
XR_001742216.1:n.1821C=
XR_427718.2:n.1907C=
XR_948290.2:n.1673C=
XR_948291.2:n.1901C=
NM_003060.4:c.1547C= MANE Select NP_003051.1:p.Pro516=
NM_001308122.2:c.1619C= NP_001295051.1:p.Pro540=